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111.
Matsuo Y Tahara K Sawamura M Nakamura E 《Journal of the American Chemical Society》2004,126(28):8725-8734
Selective penta-addition of a methylcopper reagent followed by addition of a phenylcopper reagent to a suitably modified synthetic intermediate results in creation of 40pi-electron systems-hoop- and bowl-shaped cyclic benzenoid compounds, [10]cyclophenacene, and dibenzo-fused corannulene derivatives. The 40pi-electron cyclophenacene derivatives have been found to be chemically stable, yellow-colored, luminescent (560 nm), and EPR-silent. X-ray crystallographic analysis provided precision structural data sets. The dibenzo-fused corannulene derivatives exhibit blue-green (460 nm) to red (649 nm) fluorescence. 相似文献
112.
Aoyagi Y Saitoh Y Ueno T Horiguchi M Takeya K Williams RM 《The Journal of organic chemistry》2003,68(18):6899-6904
Lipase TL-mediated kinetic resolution of (+/-)-5-benzyloxy-1-tert-butyldimethylsilyloxy-2-pentanol (5) at low temperature proceeded to give the corresponding (S)-alcohol 5 and (R)-acetate 6 in quantitative yields with high enantiomeric purity. The addition of bases such as pyridine, DMAP, 2,4- and 2,6-lutidines, or triethylamine considerably enhanced the rate of kinetic resolution. The alcohol (S)-5 and the acetate (R)-6 were converted to piperazic acid derivatives (R)- and (S)-3, respectively, via the intramolecular Mitsunobu reaction as a key step. 相似文献
113.
Amii H Ichihara Y Nakagawa T Kobayashi T Uneyama K 《Chemical communications (Cambridge, England)》2003,(23):2902-2903
N-Allylic difluoroenamines exhibited unusual behaviors under thermal conditions; N-allyl difluoroenamines in refluxing xylene afforded not only aza-Claisen rearrangement products, but also 2-azabicyclo[2.1.1]hexanes, whose formation could be explained via intramolecular [2+2]-cycloaddition, whilst N-prenyl difluoroenamine underwent an ene reaction to give the pyrrolidine as a sole product. 相似文献
114.
Koike R Motoyoshiya J Takaguchi Y Aoyama H 《Chemical communications (Cambridge, England)》2003,(6):794-795
A kinetic study of peroxyoxalate chemiluminescence reactions employing 2,4,6-trichlorophenyl N-aryl-N-tosyloxamates supports the 1,2-dioxetanones still bearing the eliminating group as the key intermediates that interact with the fluorophores rather than 1,2-dioxetanedione. 相似文献
115.
Yokoyama Y Shiraishi H Tani Y Yokoyama Y Yamaguchi Y 《Journal of the American Chemical Society》2003,125(24):7194-7195
Introduction of an asymmetric center to C-2 of one of the benzothiophene rings of bisbenzothienylperfluorocyclopentene results in a highly diastereoselective photochromic system. The stereogenic center bears a hydrogen atom, a methyl group, and a methoxymethoxy group. The steric as well as the electronic repulsions gave an 87-88% diastereomer excess in various solvents at room temperature with 80-85% conversion to the colored form. The enantioselective synthesis was also carried out. Upon photoirradiation in hexane, a change in optical rotation at 820 nm, where neither the open form nor the colored form absorbs light, was observed repeatedly. 相似文献
116.
Kanai M Yasumoto M Kuriyama Y Inomiya K Katsuhara Y Higashiyama K Ishii A 《Organic letters》2003,5(7):1007-1010
[reaction: see text] The highly regioselective hydrogenolysis of bis(alpha-methylbenzyl)amine derivatives proceeded with influence not from the electronic effect but from the steric effect of the trifluoromethyl substituent on the aromatic ring to provide a practical asymmetric synthesis of trifluoromethyl-substituted alpha-phenylethylamines. 相似文献
117.
Ikushima Y Hatakeda K Sato O Yokoyama T Arai M 《Angewandte Chemie (International ed. in English)》2001,40(1):210-213
118.
A. Kishimoto 《Journal of Functional Analysis》2003,200(2):281-300
When A is a unital simple AF C∗-algebra and has a unique tracial state, it is shown that the crossed product of the two-sided infinite tensor product by the shift is a tracially AF C∗-algebra. A similar result is given to the crossed product of a certain non-unital two-sided infinite tensor product by the shift. Applying a far-reaching classification result of such C∗-algebras by H. Lin, we obtain an example of a one-parameter automorphism group on some AF C∗-algebra which is not approximately inner, a counter-example to the AF version of the so-called Powers-Sakai conjecture [23]. 相似文献
119.
Yasutaka Takahashi Ayako Ohsugi Takeshi Arafuka Tomokazu Ohya Takayuki Ban Yutaka Ohya 《Journal of Sol-Gel Science and Technology》2000,17(3):227-238
The effects of several hydroxyketones such as acetol, actoin, -ketobutanol themselves and their combinations with monoethanolamine (MEA) or ethylenediamine (ED) on the stabilization of titanium tetraisopropoxide (TTIP) in isopropanol solution are examined. Acetoin itself and the imine derivatives of acetol and acetoin were found to show extraordinarily strong stabilizing effect for the alkoxide. The properties including the crystal modifications and refractive index of TiO2 films that were dip-coated using each stabilized solution are examined and discussed in comparison with those of the films obtained from the diethanolamine (DEA) systems. The effect of UV-light irradiation to the gel films on the crystallization of TiO2 is also examined and discussed. 相似文献
120.
Yutaka Ono 《Tetrahedron letters》2006,47(4):421-424
The epoxidation of alkenylphosphorus compounds with hydrogen peroxide was systematically studied, revealing that while alkenylphosphine oxides failed to produce the corresponding epoxides, alkenylphosphonates, or phosphinates having a phenyl group at α-position reacted with H2O2/K2CO3 or alkenylphosphonic acids or phosphinic acids having an aliphatic group at α- or β-positions reacted with H2O2/Na2WO4/Et3N to produce high yields of the corresponding epoxides. 相似文献